Maryam K. Al Badi
Muscat, MA, Oman
Last Updated: 09/26/2026
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Found 10 publications
XLH Matters 2024 GCC Edition: Insights and Recommendations to Improve Outcomes for People Living With XLH in the Gulf Region.
Journal: Clinical medicine insights. Endocrinology and diabetes
Published: December 19, 2025
Phenotypic diversity in autosomal recessive hypophosphatemic rickets type 2.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: June 30, 2025
Two cases of neonatal hyperglycemia caused by a homozygous COQ9 stop-gain variant.
Journal: Journal of diabetes investigation
Published: December 11, 2024
A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population.
Journal: Journal of the Endocrine Society
Published: July 14, 2021
Case Report: Investigation and molecular genetic diagnosis of familial hypomagnesaemia.
Journal: F1000Research
Published: November 22, 2019
Higher serum alkaline phosphatase activity in infants born to vitamin D-deficient mothers.
Journal: Archives of osteoporosis
Published: December 30, 2018
Testosterone- and Cortisol-secreting Oncocytic Adrenocortical Adenoma in the Pediatric Age-group.
Journal: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
Published: February 11, 2018
Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 13, 2017
Genetic mutations associated with neonatal diabetes mellitus in Omani patients.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: July 20, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026